112970-65-7

Basic information

• Product Name: 1H-Indole, 4-methyl-1-[(4-methylphenyl)sulfonyl]-
• CAS NO: 112970-65-7
• Molecular Formula: C16H15NO2S
• Molecular Weight: 285.367
• Mol File: 112970-65-7.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: 1H-Indole, 4-methyl-1-[(4-methylphenyl)sulfonyl]-(CAS DataBase Reference)
• NIST Chemistry Reference: 1H-Indole, 4-methyl-1-[(4-methylphenyl)sulfonyl]-(112970-65-7)
• EPA Substance Registry System: 1H-Indole, 4-methyl-1-[(4-methylphenyl)sulfonyl]-(112970-65-7)

Safety Data

• Hazardous Substances Data: 112970-65-7(Hazardous Substances Data)

Upstream product

• 98203-15-7 2-bromo-3-methyl-N-tosylaniline 
• 76605-82-8 6-methyl-cyclohex-1-en-1-yl trifluoromethanesulfonate 
• 941-55-9 4-toluenesulfonyl azide 
• 65691-69-2 1-ethynyl-6-methylcyclohex-1-ene 
• 16096-32-5 4-methyl-1H-indole 
• 98-59-9 p-toluenesulfonyl chloride 
• 17639-64-4 N-p-toluenesulfonylpyrrole 
• 41085-43-2 2-bromo-3-nitrotoluene 
• 54879-20-8 2-bromo-3-methylaniline 
• 570-24-1 2-Methyl-6-nitroaniline 
• 894810-44-7 N-allyl-4-methyl-N-(3-methyl-2-vinyl-phenyl)-benzenesulfonamide 
• 112970-52-2 N-p-toluenesulfonyl-2-ethenyl-3-methylaniline 
• 129667-00-1 4-[1,3]Dioxolan-2-yl-2-[1-(toluene-4-sulfonyl)-1H-pyrrol-3-yl]-butan-2-ol 
• 106058-85-9 1-(1-tosyl-1H-pyrrol-3-yl)ethan-1-one 

Downstream Products

• 16096-32-5 4-methyl-1H-indole 
• 1349111-18-7 C₁₉H₁₉NO₃S 
• 1349111-22-3 C₂₂H₂₅NO₃S 
• 1262322-65-5 C₁₈H₁₇NO₃S 
• 142958-94-9 2-(4-Methyl-1H-indol-1-yl)benzonitrile 
• 887338-39-8 3-bromo-4-methyl-1-(toluene-4-sulfonyl)-1H-indole 

Relevant articles and documents

Silver-Catalyzed Asymmetric Dearomatization of Electron-Deficient Heteroarenes via Interrupted Barton–Zard Reaction

Herein we report a catalytic asymmetric dearomatization reaction of electron-deficient heteroarenes with α-substituted isocyanoacetates through an interrupted Barton–Zard reaction. A range of optically active pyrrolo[3,4-b]indole derivatives was obtained

Conversion of cyclic ketones to 2,3-fused pyrroles and substituted indoles

A highly effective synthesis of 2,3-fused pyrroles from cyclic ketones has been achieved. The transformation includes a rhodium-catalyzed reaction of 4-alkenyl-1-sulfonyl-1,2,3-triazoles featuring an unusual 4π electrocyclization. The methodology was furt

An efficient synthesis of N-arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH

An efficient synthesis of N-arylsulfonylindoles from indoles and arylsulfonyl chlorides in the presence of triethylbenzylammonium chloride (TEBA) and NaOH at room temperature is described.